AlignerFlow LC
K号: K231817 · 2023-12-01
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申请人Voco GmbH
决定日期2023-12-01
产品代码DYH
咨询委员会DE
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决定实质等同
器械摘要
AlignerFlow LC is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2023-12-01 under 510(k) number K231817. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the AlignerFlow LC?
AlignerFlow LC is a medical device that received FDA 510(k) clearance on 2023-12-01. The listed applicant is Voco GmbH. The 510(k) number is K231817.
When did AlignerFlow LC receive FDA 510(k) clearance?
AlignerFlow LC received FDA 510(k) clearance on 2023-12-01, under 510(k) number K231817.
Who is the listed applicant for AlignerFlow LC?
The FDA 510(k) record lists Voco GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AlignerFlow LC?
The FDA product code for AlignerFlow LC is DYH.
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列明Voco GmbH为申报人的其他记录
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相关器械（代码：DYH）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
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官方来源
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